Clinical Research Department, UNICANCER, Centre François Baclesse, 3 Avenue du Général Harris, 14000, Caen, France.
Department of Medical Oncology, UNICANCER, Centre François Baclesse, 3 Avenue du Général Harris, 14000, Caen, France.
BMC Cancer. 2022 May 12;22(1):537. doi: 10.1186/s12885-022-09623-z.
Perioperative chemotherapy and surgery are a standard of care for patients with resectable gastric or gastroesophageal junction (GEJ) adenocarcinoma. However, the prognosis remains poor for this population. The FLOT (fluorouracil, leucovorin, oxaliplatin, and docetaxel) regimen is considered as the new standard chemotherapy regimen for perioperative strategy, despite associated with a 5-year overall survival rate (OS) amounting 45% following radical surgery. Immunotherapy with antibodies that inhibit PD-1/ PD-L1 interaction has recently emerged as a new treatment option with promising and encouraging early trial results for patients with advanced or metastatic gastric or GEJ adenocarcinoma. Currently, no trials have investigated the impact of perioperative immunotherapy in combination with chemotherapy for resectable gastric or GEJ adenocarcinoma.
GASPAR trial is a multicenter open-label, nonrandomized, phase II trial to evaluate the efficacy and safety of Spartalizumab in combination with the FLOT regimen as perioperative treatment for resectable gastric or GEJ adenocarcinoma. The main endpoint is the proportion of patients with pathological complete regression (pCR) in the primary tumour after preoperative treatment. Systemic treatment will include a pre-operative neoadjuvant and a post-operative adjuvant treatment, during which FLOT regimen will be administered every two weeks for 4 cycles and Spartalizumab every four weeks for 2 cycles. For patients with confirmed tumor resectability on imaging assessment, surgery will be realized within 4-6 weeks after the last dose of preoperative chemotherapy. Post-operative systemic treatment will then be initiated within 4-10 weeks after surgery. Using a Simon's two-stage design, up to 67 patients will be enrolled, including 23 in the first stage.
Currently, no trials have investigated the impact of immunotherapy in combination with FLOT chemotherapy as perioperative treatment for resectable gastric or GEJ adenocarcinoma. Some studies have suggested a change in the tumor immune micro-environment following neoadjuvant chemotherapy in this setting, reinforcing the relevance to propose a phase II trial evaluating efficacy and safety of Spartalizumab in combination with perioperative chemotherapy, with the aim of improving treatment efficacy and survival outcomes.
NCT04736485, registered February, 3, 2021.
围手术期化疗和手术是可切除胃或胃食管交界处(GEJ)腺癌患者的标准治疗方法。然而,该人群的预后仍然较差。FLOT(氟尿嘧啶、亚叶酸、奥沙利铂和多西紫杉醇)方案被认为是新的围手术期标准化疗方案,尽管在根治性手术后 5 年总生存率(OS)达到 45%。抑制 PD-1/PD-L1 相互作用的抗体免疫疗法最近作为一种新的治疗选择出现,对于晚期或转移性胃或 GEJ 腺癌患者具有有前途和令人鼓舞的早期试验结果。目前,尚无试验研究围手术期免疫治疗联合化疗治疗可切除胃或 GEJ 腺癌的影响。
GASPAR 试验是一项多中心、开放标签、非随机、II 期试验,旨在评估 Spartalizumab 联合 FLOT 方案作为可切除胃或 GEJ 腺癌围手术期治疗的疗效和安全性。主要终点是术前治疗后原发性肿瘤病理完全缓解(pCR)患者的比例。系统治疗将包括术前新辅助和术后辅助治疗,在此期间,每两周给予 FLOT 方案 4 个周期,每四周给予 Spartalizumab 2 个周期。对于影像学评估确认肿瘤可切除的患者,将在术前化疗最后一剂后 4-6 周内进行手术。术后全身治疗将在手术后 4-10 周内开始。使用 Simon 的两阶段设计,最多将招募 67 名患者,其中第一阶段包括 23 名患者。
目前,尚无试验研究免疫疗法联合 FLOT 化疗作为可切除胃或 GEJ 腺癌围手术期治疗的影响。一些研究表明,在这种情况下,新辅助化疗后肿瘤免疫微环境发生了变化,这强化了提出一项评估 Spartalizumab 联合围手术期化疗疗效和安全性的 II 期试验的相关性,旨在提高治疗效果和生存结果。
NCT04736485,于 2021 年 2 月 3 日注册。